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FDA 510(k)

OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT

K-Number: K801641 · 1980-07-28

ApplicantOhio Medical Products
Decision Date1980-07-28
Product CodeDTS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Medical Products. It received FDA 510(k) clearance on 1980-07-28 under 510(k) number K801641. The device is classified under product code DTS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT?

OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Ohio Medical Products. The 510(k) number is K801641.

When did OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT receive FDA 510(k) clearance?

OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801641.

Who is the listed applicant for OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT?

The FDA 510(k) record lists Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT?

The FDA product code for OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT is DTS.

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Other records listing Ohio Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K841733OHIO WASTE GAS SCAVENGING RESERVOIRK842003OHIO WASTE GAS SCAVENGING INTERFACEK840356OHIO UNITROL II ANESTHESIA GAS MACHINEK841274BAG-TO-VENTILATOR SELECTOR VALVEK840967OHIO HEAT REFLECTING PATCHK840857OHIO 3000 INFANT WARMER SYSTEM

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Related Devices (Code: DTS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K053021ESTECH CLEARVIEW MV ATRIAL DEPRESSOREstech, Inc.K982891CALIFORNIA MEDICAL LABORATORIES INC. STANDARD AND SMALL RIGID TIP SUCTION WANDSCalifornia Medical Laboratories, Inc.K963756IBC CARDIAC SUCTION WARDInternational Biophysics Corp.K905008FLEXIBLE INTRACARDIAC SUCTION DEVICEGish Biomedical, Inc.K900339HAND-HELD INTRACARDIAC SUCKERS W/ERGONOMIC HANDLESShiley, Inc.K891906ROBICSEK INTRACARDIAC SUCTION WANDGish Biomedical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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